Why You Should Consider Outsourcing Your Cloud Vendor Qualification Learn why outsourcing cloud vendor qualification saves time, reduces risk, and ensures compliance with FDA standards. Download the white paper now. Various Authors - February 15, 2022 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Regulatory
Q&A: SaMD Regulations and Compliant Development Environments Blog article written from the Q&A during the SaMD Regulations and Compliant Development Environments webinar. Various Authors - February 13, 2022 Blogs Medical Device Information Technology, Regulatory
Complaint Handling Integration with Salesforce Improves Patient Care Case study on Complaint Handling Integration with Salesforce Improves Patient Care. Jim Macdonell - February 12, 2022 Case Studies Medical Device Information Technology, Regulatory
The Origins of UDI Blog article topic: The Origins of UDI. Jay Crowley - February 11, 2022 Blogs Medical Device Manufacturing, Regulatory, Safety
GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Blog article topic: GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Diane Gleinser - February 10, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Regulatory
Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance On-demand webinar topic: Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Regulatory
